Human genes for glycogen storage disease VI
Glycogen storage disease VI [DOID:2754]
A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation.
Synonyms: glycogen storage disease VI, DOID:2754, glycogen storage disease VIs, glycogen storage disease type VI, hepatic glycogen phosphorylase deficiency ...
Linkouts: OMIM